Terms: = Liver cancer AND SH2B3, LNK, 10019, ENSG00000111252, Q9UQQ2
3 results:
1. Rare sh2b3 coding variants in lupus patients impair B cell tolerance and predispose to autoimmunity.
Zhang Y; Morris R; Brown GJ; Lorenzo AMD; Meng X; Kershaw NJ; Kiridena P; Burgio G; Gross S; Cappello JY; Shen Q; Wang H; Turnbull C; Lea-Henry T; Stanley M; Yu Z; Ballard FD; Chuah A; Lee JC; Hatch AM; Enders A; Masters SL; Headley AP; Trnka P; Mallon D; Fletcher JT; Walters GD; Šestan M; Jelušić M; Cook MC; Athanasopoulos V; Fulcher DA; Babon JJ; Vinuesa CG; Ellyard JI
J Exp Med; 2024 Apr; 221(4):. PubMed ID: 38417019
[TBL] [Abstract] [Full Text] [Related]
2. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.
Hindy G; Dornbos P; Chaffin MD; Liu DJ; Wang M; Selvaraj MS; Zhang D; Park J; Aguilar-Salinas CA; Antonacci-Fulton L; Ardissino D; Arnett DK; Aslibekyan S; Atzmon G; Ballantyne CM; Barajas-Olmos F; Barzilai N; Becker LC; Bielak LF; Bis JC; Blangero J; Boerwinkle E; Bonnycastle LL; Bottinger E; Bowden DW; Bown MJ; Brody JA; Broome JG; Burtt NP; Cade BE; Centeno-Cruz F; Chan E; Chang YC; Chen YI; Cheng CY; Choi WJ; Chowdhury R; Contreras-Cubas C; Córdova EJ; Correa A; Cupples LA; Curran JE; Danesh J; de Vries PS; DeFronzo RA; Doddapaneni H; Duggirala R; Dutcher SK; Ellinor PT; Emery LS; Florez JC; Fornage M; Freedman BI; Fuster V; Garay-Sevilla ME; García-Ortiz H; Germer S; Gibbs RA; Gieger C; Glaser B; Gonzalez C; Gonzalez-Villalpando ME; Graff M; Graham SE; Grarup N; Groop LC; Guo X; Gupta N; Han S; Hanis CL; Hansen T; He J; Heard-Costa NL; Hung YJ; Hwang MY; Irvin MR; Islas-Andrade S; Jarvik GP; Kang HM; Kardia SLR; Kelly T; Kenny EE; Khan AT; Kim BJ; Kim RW; Kim YJ; Koistinen HA; Kooperberg C; Kuusisto J; Kwak SH; Laakso M; Lange LA; Lee J; Lee J; Lee S; Lehman DM; Lemaitre RN; Linneberg A; Liu J; Loos RJF; Lubitz SA; Lyssenko V; Ma RCW; Martin LW; Martínez-Hernández A; Mathias RA; McGarvey ST; McPherson R; Meigs JB; Meitinger T; Melander O; Mendoza-Caamal E; Metcalf GA; Mi X; Mohlke KL; Montasser ME; Moon JY; Moreno-Macías H; Morrison AC; Muzny DM; Nelson SC; Nilsson PM; O'Connell JR; Orho-Melander M; Orozco L; Palmer CNA; Palmer ND; Park CJ; Park KS; Pedersen O; Peralta JM; Peyser PA; Post WS; Preuss M; Psaty BM; Qi Q; Rao DC; Redline S; Reiner AP; Revilla-Monsalve C; Rich SS; Samani N; Schunkert H; Schurmann C; Seo D; Seo JS; Sim X; Sladek R; Small KS; So WY; Stilp AM; Tai ES; Tam CHT; Taylor KD; Teo YY; Thameem F; Tomlinson B; Tsai MY; Tuomi T; Tuomilehto J; Tusié-Luna T; Udler MS; van Dam RM; Vasan RS; Viaud Martinez KA; Wang FF; Wang X; Watkins H; Weeks DE; Wilson JG; Witte DR; Wong TY; Yanek LR; ; ; ; Kathiresan S; Rader DJ; Rotter JI; Boehnke M; McCarthy MI; Willer CJ; Natarajan P; Flannick JA; Khera AV; Peloso GM
Am J Hum Genet; 2022 Jan; 109(1):81-96. PubMed ID: 34932938
[TBL] [Abstract] [Full Text] [Related]
3. Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.
Lindström S; Wang L; Smith EN; Gordon W; van Hylckama Vlieg A; de Andrade M; Brody JA; Pattee JW; Haessler J; Brumpton BM; Chasman DI; Suchon P; Chen MH; Turman C; Germain M; Wiggins KL; MacDonald J; Braekkan SK; Armasu SM; Pankratz N; Jackson RD; Nielsen JB; Giulianini F; Puurunen MK; Ibrahim M; Heckbert SR; Damrauer SM; Natarajan P; Klarin D; ; de Vries PS; Sabater-Lleal M; Huffman JE; ; Bammler TK; Frazer KA; McCauley BM; Taylor K; Pankow JS; Reiner AP; Gabrielsen ME; Deleuze JF; O'Donnell CJ; Kim J; McKnight B; Kraft P; Hansen JB; Rosendaal FR; Heit JA; Psaty BM; Tang W; Kooperberg C; Hveem K; Ridker PM; Morange PE; Johnson AD; Kabrhel C; Trégouët DA; Smith NL
Blood; 2019 Nov; 134(19):1645-1657. PubMed ID: 31420334
[TBL] [Abstract] [Full Text] [Related]
